| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104729-49104948 | Rare:85; Clinvar (benign):3 | ||||
| chr3:49120879-49121187 | Rare:79; Clinvar:1 | ||||
| chr3:49132947-49133167 | Rare:41; Clinvar:2 | ||||
| chr3:49166286-49166426 | Common:1; Rare:37 | ||||
| chr3:49339994-49340132 | Common:2; Rare:64 | ||||
| chr3:49358274-49358414 | Common:2; Rare:84 | ||||
| chr3:49411820-49412213 | Common:1; Rare:125 | ||||
| chr3:49429230-49429374 | Rare:40 | ||||
| chr3:49470004-49470319 | Common:1; Rare:94 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 | ||||
| chr3:49688643-49688745 | Common:1; Rare:34 | ||||
| chr3:49689460-49689631 | Rare:50 | ||||
| chr3:49786528-49786778 | Rare:76 | ||||
| chr3:50267402-50267687 | Common:2; Rare:87 | ||||
| chr3:50268988-50269267 | Common:1; Rare:79 |